A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516839



Internal ID22574802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:81983886..81996208hg38UCSC Ensembl
chrX:81239335..81251657hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3812323
hg1912323
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977966
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516839
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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